A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633769



Internal ID6673888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22902613..22903539hg38UCSC Ensembl
Innerchr14:22902613..22903539hg38UCSC Ensembl
Outerchr14:22902377..22903764hg38UCSC Ensembl
chr14:23371822..23372748hg19UCSC Ensembl
Innerchr14:23371822..23372748hg19UCSC Ensembl
Outerchr14:23371586..23372973hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38927
hg19927
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14935056
SamplesHG01073
Known GenesRBM23
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633769
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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